Wide range of services for your clinical site

By alleviating the administrative burden associated with trial conduct, Pulse provides clinical trial sites the opportunity to prioritise their patient recruitment and care.

Project Management and Monitoring Support

Provide CRA, PM and CTM support for sponsors and CROs to ensure compliant and optimum study execution.

Ethics and Governance

IRB/IEC (HREC and RGO) submissions (commercially sponsored, collaborative and investigator-initiated)

Budgets and Contracts

Full life cycle Budget negotiations and contract negotiation until execution.

Document and Worksheet Development

Development of informed consent forms and drafting source document worksheets based on CRF

Participant Payment/Invoice Reconciliation

Reconciling the payment for participant visits against the protocol to ensure accuracy in invoicing

Feasability Management & Study Brokering Service

Sourcing of studies from CROs/Sponsors and full lifecycle managment from CDA to site seleciton

Regulatory Oversight

Complete, review all CTN and safety notifications to the TGA

Essential Document Collection & Collation

Essential document collection & collation of all study documented needed for site activation

Study Managment and Comms

Other administration and sponsor communication throughout study start-up.

Our process

Get started quickly and see how we can reduce your administrative burden.

1

Intro call

60 min

Discuss your study’s details and how Pulse can best serve you. Pulse can tailor a package to meet your bespoke needs.

2

Execute

7 days

Following the signing of an agreement, study activity will commence as per the discussed plan and timeline.

3

Review & Optimise

3 Months

After first study lifecycle is complete, Pulse will initiate a feedback and optimisation cycle to enhance performance on future studies.

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Blogs

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I want to start conducting Clinical Trials: A Guide for Australian Clinics

Discover the transformative journey towards conducting clinical trials within Australian clinics with our expert guide. This comprehensive roadmap is designed for general practitioners, specialists, and clinic administrators eager to contribute to groundbreaking medical research and improve patient care.

Enhancing Clinical Trial Success through Vendor Partnerships

Unlocking Clinical Trial Efficiency: Outsourcing Study Start-Up Activities in Australia

In Australia's rapidly evolving clinical trial landscape, outsourcing study start-up activities offers a strategic solution for enhancing efficiency and reducing costs. This approach leverages specialized expertise to streamline processes, expedite study initiation, and focus resources on core research activities, ultimately accelerating the delivery of life-changing treatments.

Supercharge you study start up with Pulse

Empowering Clinical Sites To Be Patient-Centric By Minimising Administrative Burden.

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